NDC 68828-285 Jafra Royal Luna Bright Kit
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68828-285?
What are the uses for Jafra Royal Luna Bright Kit?
Which are Jafra Royal Luna Bright Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Jafra Royal Luna Bright Kit Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- LAUROYL LYSINE (UNII: 113171Q70B)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- DOCOSANOL (UNII: 9G1OE216XY)
- ARGININE (UNII: 94ZLA3W45F)
- LEVOMENOL (UNII: 24WE03BX2T)
- SHEA BUTTER (UNII: K49155WL9Y)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALLANTOIN, (+)- (UNII: XDK458E1J9)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- PEG-100 STEARATE (UNII: YD01N1999R)
- DULSE (UNII: 7832HOY4ZQ)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- ROYAL JELLY (UNII: L497I37F0C)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PEG-20 SORBITAN ISOSTEARATE (UNII: X958PZJ9ON)
- COCOA (UNII: D9108TZ9KG)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".